Date: | September 14, 2017 - 9:00am - September 15, 2017 - 6:00pm |
Timezone: | (GMT-05:00) Eastern Time (US & Canada) |
Location: | CA, United States |
Website for Event: | http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901150SE... |
Topic: | Sales Management Training |
Description: | Course "Compliance Boot Camp" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion. Overview: This 2-day seminar will cover the essentials of compliance for medical device companies. An efficient and effective quality system can be a competitive advantage for companies by leading to improved quality and compliance as well as optimizing the cost of quality. This "Compliance Boot Camp" will get you started in setting up just such a Quality System. We'll discuss the "case for quality" and how you can use compliance, not as an end itself, but as a means to improved quality and reduced cost of non-compliance. In this seminar, we will discuss: • Regulatory Expectations Why should you attend: This seminar will help you understand regulatory requirements and how to translate them into a quality system that is both effective and efficient. You'll learn how to plan, structure, and implement a quality system specific for your business needs. We'll explore the capabilities that every medical device company needs to ensure quality products and a compliant quality system. We'll discuss how to create a quality strategy and plans. Will discuss methods to identify, prioritize, and analyze risks. Then will move on to continuous improvement, six sigma, and Corrective and Preventive Action to address issues within your Quality System. You'll learn how to effectively communicate and escalate risk as well as monitor performance and progress. Learning Objectives: This 2-day seminar will cover the following areas: Who will benefit: • Quality Systems Specialists Agenda: Day 1 Schedule Lecture 1: Day 2 Schedule Lecture 1: Speaker: Susanne Manz, MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and Six Sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities. While at industry leaders like GE, J&J, and Medtronic, Susanne worked in various world-wide roles including Executive Business Consultant, Worldwide Director of Quality Engineering, Worldwide Director of Design Quality, and Director of Corporate Compliance. She has traveled extensively throughout the world conducting audits and helping companies to understand and improve their Quality Management Systems. Susanne is a Presidential Scholar and has a BS in Biomedical Engineering and an MBA from the University of NM. Location: San Diego, CA Date: September 14th & 15th, 2017 and Time: 9:00 AM to 6:00 PM Price: Register now and save $200. (Early Bird) Sponsorship Program benefits for “Quality Assurance Auditing for FDA Regulated Industry” seminar Contact us today! NetZealous LLC DBA GlobalCompliancePanel Registration Link -http://www.globalcompliancepanel.com/control/globalseminars/~product_id=901150SEMINAR?selfgrowth-September-2017-SEO Follow us on LinkedIn: https://www.linkedin.com/company/globalcompliancepanel/ |
Contact Name: | Event Manager |
Contact Email: | john.robinson@globalcompliancepanel.com |
Contact Phone: | 800-447-9407 |